Nonalcoholic fatty liver disease (NAFLD) affects approximately 30% adults in the US. NAFLD initially manifests hepatic steatosis and progresses to nonalcoholic steatohepatitis (NASH), fibrosis, and even cirrhosis or hepatocellular carcinoma. Liver fibrosis, a condition of elevated accumulation of extracellular matrix in the liver, is a strong indicator of NASH severity. In most NASH patients, environmental factors such as high-calorie diets and sedentary lifestyle are primary contributors to the disease development. Those environmental cues often modulate epigenetic and transcription factors to acquire long-term effects. In our preliminary study, we have identified Sirtuin 6 (Sirt6) as a key suppressor of liver fibrosis. To further investigate the role of Sirt6 in the pathogenesis of liver fibrosis, we plan to carry out both in vitro and in vivo experiments using cell and animal models. Hepatic stellate cells are generally considered as a major contributor to the production of extracellular matrix in the liver after chronic liver injury. Therefore, we will focus on the regulation of hepatic stellate cells by Sirt6 at molecular, cellular, and tissue levels. It is expected that the proposed pathophysiological and mechanistic investigation of liver fibrosis in this application will uncover key pathways or network that is controlled by Sirt6. Moreover, the knowledge gained from this project can help develop therapeutic interventions for hepatic fibrosis.

Public Health Relevance

The proposed research in this application is highly relevant to public health because better understanding of the pathogenesis of liver fibrosis is ultimately expected to provide potential novel drug targets for the prevention and treatment of this common liver disease. The liver fibrosis can be caused by various pathogenic factors including obesity, alcohol, drug toxicity, and viral infection. Thus, this project is also relevant to the part of NIH?s mission that pertains to pursuing fundamental knowledge that will help extend healthy life and reduce the burdens of illness.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
1R01DK121925-01A1
Application #
10051527
Study Section
Xenobiotic and Nutrient Disposition and Action Study Section (XNDA)
Program Officer
Burgess-Beusse, Bonnie L
Project Start
2020-07-01
Project End
2024-06-30
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Indiana University-Purdue University at Indianapolis
Department
Biochemistry
Type
Schools of Medicine
DUNS #
603007902
City
Indianapolis
State
IN
Country
United States
Zip Code
46202